Laron syndrome with immunodeficiency (Q88878): Difference between revisions

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Latest revision as of 15:16, 15 August 2026

Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF-1 concentrations with normal or high GH concentrations, associated with immunodeficiency characterised by moderate lymphopenia which leads to recurrent infections of the skin and respiratory tract.

Language	Label	Description	Also known as
default for all languages	ID_142511578
English	Laron syndrome with immunodeficiency	Laron syndrome with immunodeficiency is characterised by severe post-natal growth retardation, delayed bone age and facial dysmorphism (prominent forehead, hypoplastic nasal bridge), and low serum IGF-1 concentrations with normal or high GH concentrations, associated with immunodeficiency characterised by moderate lymphopenia which leads to recurrent infections of the skin and respiratory tract.